214104 AND nstd173 - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4365280	copy number variation	39	nstd173	human		GRCh37 chr6: 78,962,581-79,035,184 , GRCh38.p12 chr6: 78,252,864-78,325,467	LOC105377865
nsv4376609	copy number variation	40	nstd173	human		GRCh37 chr7: 141,755,372-141,789,964 , GRCh38.p12 chr7: 142,055,572-142,090,164 , GRCh38.p12 chr7\|NT_187562.1: 17,452-52,044	MGAM
nsv4371460	copy number variation	1	nstd173	human		GRCh37 chr1: 72,773,260-72,802,491 , GRCh38.p12 chr1: 72,307,577-72,336,808 , GRCh38.p12 chr1\|NW_018654707.1: 19,844-49,073	LOC105378797
nsv4387719	copy number variation	1	nstd173	human		GRCh37 chr5: 110,417,792-110,456,263 , GRCh38.p12 chr5: 111,082,094-111,120,565	WDR36
nsv4387002	copy number variation	71	nstd173	human		GRCh37 chr3: 128,380,595-128,412,377 , GRCh38.p12 chr3: 128,661,752-128,693,534	POU5F1P6
nsv4386511	copy number variation	1	nstd173	human		GRCh37 chr13: 69,220,603-69,268,719 , GRCh38.p12 chr13: 68,646,471-68,694,587	RPL12P34, RN7SL761P
nsv4376418	copy number variation	25	nstd173	human		GRCh37 chr12: 2,235,941-2,258,023 , GRCh38.p12 chr12: 2,126,775-2,148,857 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-491,001	LOC107984131, CACNA1C
nsv4370238	copy number variation	91	nstd173	human		GRCh37 chr4: 69,367,141-69,485,978 , GRCh38.p12 chr4: 68,501,423-68,620,260	LOC100422402, UGT2B17, 2 more genes
nsv4383855	copy number variation	44	nstd173	human		GRCh37 chrX: 103,259,181-103,312,921 , GRCh38.p12 chrX: 104,004,609-104,058,356	H2BW2, LOC107985662, 1 more genes
nsv4377227	copy number variation	3	nstd173	human		GRCh37 chr16: 75,537,696-75,575,947 , GRCh38.p12 chr16: 75,503,798-75,542,049	CHST5, TMEM231P1, 1 more genes
nsv4367001	copy number variation	197	nstd173	human		GRCh37 chr14: 74,001,111-74,024,031 , GRCh38.p12 chr14: 73,534,407-73,557,327	NT5CP2, ACOT1, 1 more genes
nsv4374875	copy number variation	271	nstd173	human		GRCh37 chr6: 67,009,023-67,051,189 , GRCh38.p12 chr6: 66,299,130-66,341,296	0
nsv4381531	copy number variation	237	nstd173	human		GRCh37 chr2: 34,701,643-34,737,163 , GRCh38.p12 chr2: 34,476,576-34,512,096	0
nsv4383282	copy number variation	1	nstd173	human		GRCh37 chr14: 22,420,174-22,975,728 , GRCh38.p12 chr14: 21,951,951-22,506,743	TRAV29DV5, TRAJ56, 76 more genes
nsv4385422	copy number variation	1	nstd173	human		GRCh37 chr9: 108,981,418-109,189,271 , GRCh38.p12 chr9: 106,219,137-106,426,990	0
nsv4366173	copy number variation	39	nstd173	human		GRCh37 chr7: 142,266,307-142,475,287 , GRCh38.p12 chr7: 142,618,685-142,732,123 , GRCh38.p12 chr7\|NT_187562.1: 656,734-770,033	TRBV27, TRBV24-1, 16 more genes
nsv4370390	copy number variation	11	nstd173	human		GRCh37 chr14: 106,536,991-106,667,115 , GRCh38.p12 chr14: 106,112,755-106,210,472 , GRCh38.p12 chr14\|NT_187600.1: 580,524-678,241	IGHV3-20, IGHV1-18, 15 more genes
nsv4384530	copy number variation	28	nstd173	human		GRCh37 chr7: 38,319,296-38,387,020 , GRCh38.p12 chr7: 38,279,695-38,347,419	TRGVA, , 12 more genes

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